O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester

Base Information

Chemical Name:O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester
CAS No.:1417715-03-7
Molecular Formula:C₂₆H₂₈Br₂O₈
Molecular Weight:628.312
Hs Code.:

Synonyms:O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester

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Chemical Property of O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester

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Technology Process of O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester

There total 1 articles about O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 79.0%

: 4870-65-9,31302-84-8
2-bromophenylacetic acid

: 2217-15-4
L-(+)-diisopropyl tartrate

: 1417715-03-7
O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; for 10h;
DOI:10.5012/bkcs.2012.33.11.3853

Reference yield: 98.0%

: 1417715-03-7
O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester

: 140-28-3,87170-83-0
N,N'-Dibenzylethylenediamine

: 1327310-96-2
1,4-dibenzyl-(S)-3-phenyl-2-piperazinone

: 1327310-54-2
1,4-dibenzyl-(R)-3-phenyl-2-piperazinone

Guidance literature:: With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 12h; enantioselective reaction;
DOI:10.5012/bkcs.2012.33.11.3853

Reference yield: 96.0%

: 1417715-03-7
O,O'-di(α-bromo-α-phenylacetyl)-L-tartaric acid diisopropyl ester

: 3171-45-7
4,5-dimethyl-1,2-phenylenediamine

: (3S)-6,7-dimethyl-3-phenyl-3,4-dihydroquinoxalin-2(1H)-one

: (3R)-6,7-dimethyl-3-phenyl-3,4-dihydroquinoxalin-2(1H)-one

Guidance literature:: With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 12h; enantioselective reaction;
DOI:10.5012/bkcs.2012.33.11.3853